Variants linked to Bipolar Disorder

Continuously updated · newest added Oct 23, 2026

95 positions on this site are linked to Bipolar Disorder, out of 111,351 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Sensitive

Bipolar I disorder

near RASGRP1 · rs6495988

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Sensitive

Bipolar I disorder

IFT81 · rs12315174

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Sensitive

Bipolar I disorder

CACNA1C · rs11062170

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Sensitive

Bipolar I disorder

SHANK2 · rs12575685

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Sensitive

Bipolar I disorder

CACNB2 · rs4748468

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Sensitive

Bipolar I disorder

near CACNA1B · rs11137399

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Sensitive

Bipolar I disorder

PLEC · rs6993953

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Sensitive

Bipolar I disorder

near H3C8 · rs55706012

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Sensitive

Bipolar I disorder

near ZMAT2 · rs6875495

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Sensitive

Bipolar I disorder

ADCY2 · rs78308718

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Sensitive

Bipolar I disorder

PLEC · rs57957974

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Sensitive

Bipolar I disorder

MAD1L1 · rs10950456

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Sensitive

Bipolar I disorder

MEF2BNB-MEF2B · rs111444407

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Sensitive

Binge eating behaviour in bipolar disorder

PRR5 · rs726170

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Sensitive

Bipolar disorder

MAD1L1 · rs4332037

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Sensitive

Bipolar disorder

MAD1L1 · rs4236274

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Sensitive

Bipolar disorder

NFIX · rs4926298

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Sensitive

Bipolar disorder lithium response (continuous) or schizophrenia

HLA · rs209474

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Sensitive

Bipolar disorder lithium response (categorical) or schizophrenia

MEF2C · rs324899

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Sensitive

Bipolar disorder or attention deficit hyperactivity disorder

TAF9BP2 · rs7089973

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Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.